A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4070n106



Internal ID22797898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76121810..76122122hg38UCSC Ensembl
chr9:78736726..78737038hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121419, nsv1130176
SamplesKWS2
Known GenesPCSK5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4070n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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